Lipophilic statins antagonistically alter the major epithelial-to-mesenchymal transition signaling pathways in breast cancer stem–like cells via inhibition of the mevalonate pathway

Resistance to therapies, recurrence, and metastasis remain challenging issues for breast cancer patients, particularly for triple-negative and breast cancer stem cells. The activation of the epithelial-to-mesenchymal transition (EMT) plays an indispensable role in the poor prognosis of those types. The accumulating proofs indicated that the mevalonate pathway crucially mediates a poor prognosis. Here, the effects of lipophilic 3-hydroxy-3-methyl-glutaryl-coenzyme A inhibitors, atorvastatin, lovastatin, and simvastatin, were investigated on expression and function of a selected profile of EMT-related genes in breast cancer stem–like cells. A nontoxic dose of statins (5 μM for 4 days) significantly (P < 0.05 and >2-fold change) altered expression of 50 of 71 studied genes with a shared cluster of 37 genes that are coding chief operator of signaling pathways in Hippo, Notch, Wnt, proliferation, invasion, angiogenesis, and cell death. They also significantly decreased the levels of Yap/Taz proteins and shifted the expression of vimentin/E-cadherin in favor of induction of differentiation. Statins significantly chemosensitized the treated cells to doxorubicin and also reduced in vitro migration of the cells. Whereas lovastatin and simvastatin significantly decreased the expression of CD44, atorvastatin drastically increased CD24 and caused more wide-ranging impacts. In summary, the statins hold back the process of EMT by the antagonizing of EMT-promoting pathways. High degree of overlapping findings is supportive of the central role of the mevalonate pathway in cancer stem–like cells, but further studies are required to find the optimized chemical structure for the maximum abrogation of orchestrated EMT pathways.     

Conditioned media from human pluripotent stem cell-derived cardiomyocytes inhibit the growth and migration of lung cancer cells

Conditioned media (CM) from various cell types contain significant levels of paracrine factors. Recently, therapeutic properties of CM derived from stem cells have been revealed. Based on the fact that heart cancer is extremely rarely, we hypothesized that the CM obtained from human pluripotent stem cell-derived cardiomyocytes might inhibit cancer cell growth and survival. To this end, lung cancer cell line A549 along with human foreskin fibroblasts (HFF) were treated with serial concentrations of cardiomyocyte CM (CCM) or fibroblast CM (FCM). We found that CCM markedly reduced the viability of lung cancer cells, while FCM did not compromise the viability of neither cancer cells nor HFF cells. Furthermore, we determined an optimized CCM concentration, 30 mg/mL, at which the growth, clonogenicity, and migration of A549 and Calu6 lung cancer cell lines were substantially impaired, whereas FCM did not influence these properties. Moreover, lung cancer cells exhibited cell cycle regulation upon treatment with CCM and the rate of apoptosis was markedly increased by cardiomyocyte CM in both lung cancer cell lines tested. Finally, in response to CCM treatment, A549 and Calu6 cells expressed lower levels of antiapoptotic and stemness genes, but higher levels of proapoptotic genes. In conclusion, this study provides cellular and molecular evidence for the antitumor ability of secretome obtained from stem cell-derived cardiomyocytes.     

Fine structure of cultured epithelial cells derived from voided urine of normal adults

Cultures of epithelial cells can be initiated with the sediment of voided urine of normal adults. Tightly or loosely packed colonies were formed by cells of diverse morphologic configuration. Ultrastructural studies revealed that the proliferating cells formed abundant desmosomes, imperfectly formed tight junctions and lamina densa, all typical of epithelial cells. Some cells were lined by the characteristic asymmetric unit membrane, thus confirming the urothelial derivation of the cultures. Peculiar, apparently hitherto not described multivesicular bodies, seemingly of cytoplasmic origin, were observed near the surfaces of some cells. The urinary cell culture system is a potentially useful tool for diagnostic and research purposes.     

New mononuclear mercury(II) complexes of a bifunctionalized ylide containing five-membered chelate ring: Spectral and structural characterization

The reaction of a new bifunctionalized ylide, Ph₂PCH₂PPh₂C(H)C(O)(C₆H₄Cl) (2) with mercury(II) halides in equimolar ratios using dry methanol as solvent yielded the P, C-chelated complexes, {HgX₂[Ph₂PCH₂PPh₂C(H)C(O)(C₆H₄Cl)]} where X = Cl (3), Br (4), I (5). The structures of complexes 4 and 5 have been characterized crystallographically. Single crystal X-ray analyses reveal the presence of mononuclear complexes containing Hg atom in a distorted tetrahedral environment. Characterization of the obtained compounds was also performed by elemental analysis, IR, ¹H, ³¹P, and ¹³C NMR. A theoretical study at DFT (B3LYP) level using standard CEP-31G basis set showed that the experimentally determined structure of the complex 5 is about 0.6-15.75 kcal mol⁻¹ more stable than its other bonding modes.     

Synthesis, characterization, and structural studies of mercury(II) complexes of new bidentate phosphorus ylide

The reaction of Ph₂PCH₂CH₂PPh₂ (dppe) with BrCH₂C(O)C₆H₄NO₂ (1:1.05 molar ratio) in acetone produces a mixture of the new monophosphonium salt [Ph₂PCH₂CH₂PPh₂CH₂C(O)C₆H₄NO₂]Br (1) and the diphosphonium salt [NO₂C₆H₄C(O)CH₂PPh₂CH₂CH₂PPh₂CH₂C(O)C₆H₄NO₂]Br₂ (2). Compound 2 was insoluble in acetone and thus easily separated from the solution of 1. Further, by reacting both the mono- and diphosphonium salts with the appropriate bases the bidentate phosphorus ylides, [Ph₂PCH₂CH₂PPh₂CHC(O)C₆H₄NO₂] (3) and [NO₂C₆H₄C(O)CHPPh₂CH₂CH₂PPh₂CHC(O)C₆H₄NO₂] (4) were obtained. The reaction of ligand 3 with mercury(II) halides in dry methanol leads to the formation of the P,P-coordinated monomeric complexes {HgX₂(Ph₂PCH₂CH₂PPh₂CHC(O)C₆H₄NO₂)₂} [X = Cl (5), Br (6), I (7)]. The structure of complex 7 being unequivocally determined by single crystal X-ray diffraction techniques. Characterization of these species was also performed by elemental analysis, IR spectroscopy and ¹H, ³¹P, and ¹³C NMR techniques. These analyses being consistent with a 2:1 stoichiometry ylide/Hg(II) for compounds 5 through 7. Results obtained from theoretical studies are also consistent with a product in which two ylides are coordinated to the Hg(II) center through their phosphine groups, being this product the most stable among all the possible products.     

Screening for transient biological interactions as applied to albumin ligands: a new concept for drug discovery

The notion that many biological interactions are based on transient binding (dissociation constants (K(d)) in the range of 10-0.01 mM) is familiar, yet the implications for biological sciences have been realized only recently. An important area of biological sciences is drug design, where the traditional "lock and key" view of binding has prevailed and drug candidates are usually selected on their merits as being tight binders. However, the rationale that transient interactions are of importance for drug discovery is slowly gaining acceptance. These interactions may relate not only to the desired target interaction but also to unwanted interactions creating, for example, toxicity problems. Here we demonstrate, in a high-throughput screening format, affinity selection of weak binders to a model target of albumin by zonal retardation chromatography. It is perceived that this approach can define the "transient drug" as a complement to current drug discovery procedures.     

Pravastatin reverses the membrane cholesterol reorganization induced by myocardial infarction within lipid rafts in CD14(+)/CD16(-) circulating monocytes

Large numbers of monocytes are recruited in the infarcted myocardium. Their cell membranes contain cholesterol-rich microdomains called lipids rafts, which participate in numerous signaling cascades. In addition to its cholesterol-lowering effect, pravastatin has several pleiotropic effects and is widely used as secondary prevention treatment after myocardial infarction (MI). The aim of this study was to investigate the effects of pravastatin on the organization of cholesterol within monocyte membrane rafts from patients who had suffered myocardial infarction. Monocytes from healthy donors and acute MI patients were cultured with or without 4μM pravastatin. Lipid rafts were extracted by Lubrol WX, caveolae and flat rafts were separated using a modified sucrose gradient. Cholesterol level and caveolin-1 expression in lipid rafts were determined. In healthy donors, cholesterol was concentrated in flat rafts (63±3 vs 13±1%, p<0.001). While monocytes from MI patients presented similar cholesterol distribution in both caveolae and flat rafts. Cholesterol distribution was higher in flat rafts in healthy donors, compared to MI patients (63±3 vs 41±2%, p<0.001), with less distribution in caveolae (13±1 vs 34±2%, p<0.001). Pravastatin reversed the cholesterol distribution in MI patients cells between flat rafts (41±2 vs 66±3%, p<0.001) and caveolae (34±2 vs 18±1%, p<0.001). In conclusion, MI redistributes cholesterol from flat rafts to caveolae indicating monocyte membrane reorganization. In vitro pravastatin treatment restored basal conditions in MI monocytes, suggesting another effect of statins.     

Strigolactone and Methyl Jasmonate-Induced Antioxidant Defense and the Composition Alterations of Different Active Compounds in Dracocephalum kotschyi Boiss Under Drought Stress

Strigolactone (SL) and methyl jasmonate (MeJA) are one of the most important plant hormones that exert biological activity in plant responses to environmental stresses. Considering the undetected role of SL in drought tolerance and essential oil yield of medicinal plants as well as conceivable interaction among MeJA and SL, a factorial experiment was performed as a complete randomized design with three replications. Experimental factors including two irrigation regimes such as irrigation to 80% field capacity (control) and 40% field capacity (drought stress) and spraying treatments include MeJA (0 and 0.5 mM) and SL (0 and 10 μM) were applied. Treatment of plants with SL and MeJA resulted in higher tolerance to drought stress due to higher fresh and dry weights as well as lower electrolyte leakage, malondialdehyde, H₂O₂, total phenol content, total antioxidant activity and antioxidant power assay. The most important essential oil constituents of D. kotschyi included geranyl acetate (41.1–48.6%), α-pinene (16.2–18.9%), geranial (7.9–10.1%), limonene (5.5–7.0%), neral (3.5–4.1%), methyl geranate (2.3–3.3%) and geraniol (1–2.2%), the least of which was found in non-MeJA- and SL-treated plants under drought and the highest in MeJA- and SL-treated plants under drought stress. Drought tolerance of D. kotschyi became more intense and the amount of essential oil components of water stressed plants was the highest (99.2%) when these plant hormones were used together. These results suggest a cross-link between MeJA and SL in improving drought resistance and optimizing the production of essential oil of D. kotschyi.